Automation Engineer at Project Delivery Partners

, Pernambuco, Brazil -

Full Time

Start Date

Immediate

Expiry Date

26 Sep, 26

Salary

0.0

Posted On

28 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

PLC, HMI, SCADA, GAMP, FDA Guidelines, Commissioning Tests, System Validation, Analytical Skills, Project Management, Technical Support, Cross-functional Collaboration, English Proficiency, Office Suite, Negotiation Skills, Attention to Detail, Systemic Vision

Industry

Pharmaceutical Manufacturing

Description

PharmEng / Efor is a leading pharmaceutical and biopharmaceutical consulting company committed to providing innovative solutions to the challenges facing our industries. We pride ourselves on our dedication to quality, safety, and excellence in everything we do. As we continue to grow, we are looking for a highly qualified and motivated Automation Engineer to join our team. Position Title: Automation Engineer Location: Pernambuco Type of Contract: Full-Time / PJ Contract Main Responsibilities: Monitor and perform commissioning tests on automation systems for pharmaceutical manufacturing processes; Solve technical problems related to automation systems during test execution; Perform testing and validation of automation systems to ensure quality and compliance with industry standards; Provide technical support and training to customers on the use and maintenance of automation systems; Stay up to date on industry trends and advances in automation technology to continuously improve our services; Maintain project deadlines, objectives, and communications. Work closely with other team members, including engineers and technicians; Maintain accurate documentation and records of all projects and activities; Review internal documentation as needed; Ensure compliance with regulations. Perform testing and validation of automation systems. Specific Knowledge: Degree in Engineering or related fields. Solid knowledge of automation technology, including PLCs, HMIs, SCADA. Familiarity with industry norms and standards, such as GAMP and FDA guidelines; Preferably with proven experience in the Pharmaceutical Industry with more than 3 years of experience; Degree in Engineering or related fields. Solid knowledge of automation technology, including PLCs, HMIs, SCADA. Familiarity with industry norms and standards, such as GAMP and FDA guidelines; Preferably with proven experience in the Pharmaceutical Industry with more than 3 years of experience; Good communication and interpersonal skills; Knowledge of English for reading, writing, and conversation (a plus); Office Suite. Skills: Systemic vision, strong analytical skills, and attention to detail; Results-oriented; Ability to manage multiple projects and prioritize tasks effectively; Excellent communication and negotiation skills (synthesis and presentation of ideas); Ability to collaborate effectively with cross-functional teams; Knowledge: Familiarity with pharmaceutical industry regulations and best practices; Adaptability: Ability to thrive in a dynamic and fast-paced environment. Join us: If you are a dedicated and highly motivated person with a passion for ensuring the highest standards of Engineering and Quality in the Pharmaceutical Industry, we encourage you to apply. PharmEng / Efor offers a dynamic and inclusive work environment, competitive compensation, and opportunities for professional growth. Be part of our team and contribute to the success of our industry-leading solutions. PharmEng/Efor is an equal opportunity employer and welcomes applicants from all backgrounds. Thank you for your consideration and application! We review all resumes and submissions, however, due to the high volume of applications we receive, only approved candidates will be contacted.

Responsibilities

The role involves monitoring and performing commissioning tests and validation of automation systems for pharmaceutical manufacturing. It also requires providing technical support to customers and maintaining project documentation and compliance with industry regulations.